Breast cancer, Breast Cancer Awareness, Cancer, Chemo Brain, Depression, Emotional Health, Guilt, Hair loss, Hair regrowth, Health, Manchester, MRI, Periods, Tamoxifen, UK, Women's Health

Six years on: tamoxifen, guilt and life after cancer

Today marks six years since I was diagnosed with breast cancer and I’m not quite sure how to sum up everything that’s happened in the last 24 hours, let alone the last year or six years. So here’s a list, in no particular order, of random thoughts and people who have inspired me.

  1. Five-year all-clear

It took six attempts before I finally managed to have my annual MRI breast scan last Christmas. You’re supposed to have the scan at a certain point in your monthly cycle, but in 2017 my periods went quarterly (they’ve since returned), which made the whole thing quite difficult. And of course when I finally got a period, the MRI scanner broke and I only found out after I’d made the train trip from London to Manchester. But we got there in the end and after 26 phone calls I finally got the letter through the post in March to say that nothing sinister had been found. God love the NHS.

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  1. Saying goodbye to my surgeon

Due to the aforementioned difficulties in appointment scheduling with a hospital that is 200 miles away, I finally decided to move. This is easier said than done because of the emotional connection I have with Mr Sharif, the surgeon who saved my life. But I haven’t seen him once in the last two years – there was always a different doctor at every follow-up – so it was time to change. I have my first appointment with the Royal Marsden in Sutton next week and I’m hoping they’ll agree to continue with my yearly MRI scans. I never got to say goodbye to Mr Sharif and Dr Chittalia, but I love them both to bits.

  1. Tamoxifen, periods, brain fog and mental health

I’ve been on the hormone suppressant tamoxifen for five and a half years and although I haven’t suffered the horrible side effects that many of my friends have, I’ve still had plenty of unwelcome effects. One of these is what I can only refer to as a sort of brain fog or haze, where I feel spaced out, depressed and utterly exhausted, rather like a migraine without the headache. It is hard to explain to work that you are unwell when you don’t have obvious physical symptoms, and this in turn leads to feelings of guilt. But in a world that is increasingly paying attention to mental health, I’m doing my best to be kind to myself.

  1. New eyebrows

Of all the things to worry about when you have cancer, you’d think hair wouldn’t be one of them, but of course it affects the way you feel. So after five years of hating the way I looked without make-up and doing a terrible job of drawing my eyebrows in, I finally invested in the painful procedure that is microblading, or permanent eyebrow tattoos, at a brilliant place in South London called Beauty Clinic Simone. I am so pleased with the results and can’t tell you how nice it feels to wake up and feel vaguely confident with the way I look. Here’s a before and after – just bear in mind I’m wearing make-up in the after pic.

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  1. Serpentine Swim and Plymouth Half in memory of Laura Weatherall-Plane

When Laura died just over a year ago aged just 37, it affected way more people than she probably ever knew loved her. She was one of the most caring, selfless people I’d ever met and she dedicated the last few years of her life to raising money for CoppaFeel! to try and prevent young people from being diagnosed with breast cancer at the too-late stage. She ran half marathons right up until a couple of months before she died, and she never stopped. So last September, a bunch of us swam 2km in the Serpentine lake, enduring far-too-cold temperatures and mouthfuls of duck shit. Then in May this year, Laura’s husband Jon gathered a group of 150+ people to run the Plymouth Half in her honour, raising almost £20,000 for CoppaFeel’s livesaving work.

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  1. Running retirement

I’m pleased to say the Plymouth Half marked my official retirement from long-distance running, because my body has told me very firmly it’s not good for me. I’ll still do up to 10km runs and I will definitely get my nip on again because I’ve discovered open-water swimming is one of the best things ever – it’s great for mental health and, curiously, I’ve also found duck shit to be a natural face and hair mask. When I announced my official retirement on social media, I received a card in the post from Jackie Scully – quite possibly the biggest legend of the physical challenges world – saying that I had been the one to inspire her to take up running after cancer. From the woman who ran a marathon on her wedding day and has undertaken to run, cycle and swim 2018 miles in 2018, this really meant a lot.

  1. Writing a novel

Part of the reason I’ve been so busy and stressed for the last couple of years is that I’ve spent every weekend and holiday trying to write my debut novel, Single Bald Female. I am still a way off finishing it, but from September til March this year I did the Faber Academy’s (brilliant) Writing a Novel course, and yesterday the class of 2018 had our work printed in an anthology, which was sent to agents. I am incredibly excited to have already received some interest from agents and this has certainly provided added motivation to finish the book as soon as humanly possible, so watch this space.

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  1. Stylist piece

In October I wrote a piece for Stylist magazine for Breast Cancer Awareness Month. They sent a photographer round my house and she did some wonderful portraits while my cats tried to sabotage her technical equipment. The article was republished online last month on National Cancer Survivors Day, which is a weird one because it makes people living with secondary cancer feel excluded – and they are the people we need to supporting the most.

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  1. Kris Hallenga and Emily Hayward

CoppaFeel!’s founder, Kris Hallenga, is the ultimate in human beings and she has inspired me so much over the last few years – just read this post on How to glitter a turd for a brief taste of how much she is smashing it. She has been living with cancer for almost 10 years – which also means that CoppaFeel! turns 10 this year. You can support her ongoing efforts by purchasing tickets for Festifeel, which I can verify is actually awesome. Anyway, through her last blog, Kris introduced me to Emily Hayward, another magnificent human who has been YouTubing her way through a two-months-to-live cancer diagnosis and being the ultimate example of how not to feel sorry for yourself. Her wife Aisha deserves a special shout out for just being awe-inspiringly incredible.

  1. Werk werk werk

I never achieved the goal of becoming a women’s magazine editor that I set out to do five years ago, because I got side-tracked along the way when I went to intern at Restaurant magazine and heard about a job at The World’s 50 Best Restaurants that seemed like it was made for me (food + travel + writing). Four years later, I have somehow become part of an incredible family of chefs, restaurateurs, bartenders and foodies from all over the world and with every event I feel more at home. It has been one of the hardest, most stressful jobs I’ve ever done and it very much contradicts my post-cancer aim of leading a calmer life, but somehow I have stuck around because I love it and I love my team.

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Just this last week, I had the opportunity to do a live interview on stage with one of the people I most admire in the gastronomy world and whose restaurant Blue Hill at Stone Barns is simply incredible – Dan Barber. I also fluffed my way through interviews on Spanish radio and produced a 56-page book in the space of two weeks. It is not what I imagined I’d be doing four years ago but it’s pretty cool.

Needless to say, it’s been one of the most intense weeks of my life and I’m exhausted, sleep deprived and an emotional wreck, but I am SO HAPPY. All the love to everyone who’s supported me through these last six years xx

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7 thoughts on “Six years on: tamoxifen, guilt and life after cancer

  1. Adriana Tomalino says:

    Genial Laurita!Yo cumplí 9 años de tamoxifeno el 12 de junio.Yo siento los efectos colaterales: cansancio, aumento de peso.Hay que aguantar hasta los 10 años.Estuve cerca de dónde estás, fui a Liverpool en febrero x dos días, me encantó! También estuve en Londres y en Alton.Besos y abrazos!

    Enviado desde Yahoo Mail para Android El vie., 22 de jun. de 2018 a la(s) 2:57 p.m., the big scary ‘C’ word escribió: #yiv0179218053 a:hover {color:red;}#yiv0179218053 a {text-decoration:none;color:#0088cc;}#yiv0179218053 a.yiv0179218053primaryactionlink:link, #yiv0179218053 a.yiv0179218053primaryactionlink:visited {background-color:#2585B2;color:#fff;}#yiv0179218053 a.yiv0179218053primaryactionlink:hover, #yiv0179218053 a.yiv0179218053primaryactionlink:active {background-color:#11729E;color:#fff;}#yiv0179218053 WordPress.com | Laura P posted: “Today marks six years since I was diagnosed with breast cancer and I’m not quite sure how to sum up everything that’s happened in the last 24 hours, let alone the last year or six years. So here’s a list, in no particular order, of random thoughts and peo” | |

  2. Elizabeth Walker says:

    Hi Laura,
    Woooow you have achieved so much in such a small time, always knew you would do really well in what ever you did, very proud of you smart chick, keep up the great work and really hope to catch up again soon xxxxxxxxx
    xx

  3. Lisa Gilltrap says:

    Wow what a lovely post to find in my inbox as I get mentally ready for my three year post surgery/chemo check up. So happy for you. After going through this experience of breast cancer I was always concerned that the possibiloty of it coming back would hang over me like a black cloud forever and I have been pleasantly surprised that except for the few months around my check up I dont think about it much at all. What is like for you? Do you worry about it?

  4. Kayelene Leaker says:

    What excellent news. Well done. Hope you get to visit Australia eventually 😀

    Sent from my iPhone

    >

  5. Spot on about Tamoximoron . All clear. for five and a half years but those symptoms you mention are (for me) getting worse and ruining my quality of life . Be nice if there was an alternative

    Keep on keeping on
    Doug

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